Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 1975-53-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Cyano-2-methylbenzoic acid features a conjugated cyano group and methyl substituent positioned ortho to the carboxylic acid, enhancing electronic withdrawal and steric modulation. This configuration supports direct integration into pharmaceutical intermediates and functional materials via coupling reactions under standard conditions.
4-Cyano-2-methylbenzoic acid serves as a versatile building block in medicinal chemistry and materials science, enabling efficient access to functionalized aromatic scaffolds. Its ortho-substituted structure provides steric and electronic control in coupling reactions, while the carboxylic acid group facilitates direct derivatization or amide formation. The nitrile moiety offers compatibility with standard transformations such as hydrolysis or nucleophilic addition, enhancing synthetic flexibility. Bench-stable and readily purified by recrystallization, it functions reliably in multistep syntheses requiring predictable reactivity and orthogonal functional group handling.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: